Between Yes and No: B7-H4 and T cell Activation
This is done by either activating or suppressing T cells via targeting immune checkpoint receptors and their respective ligands such as the CTLA-4 receptor and the ligand PD-L1. Although treatments targeting CTLA-4 and PD-L1 have had significant success in treating cancer a portion of patients, however, do not respond1,2,3. This has created a need for alternative immunotherapies targeting different B7 molecules like B7-H4 that may be effective in treating non-responding patients.
First proposed by Lafferty and Cunningham, the hypothesis that T cells require two-signals to sustain activation is the basis for many immunotherapies4. The first signal needed for activation is the binding of MHC I/II molecules present on antigen presenting cells (APCs) to the T cell receptor5. While this activates key signaling pathways like PI3K-Akt-MTORC1, MAPK and NFkB, it is by itself not enough to maintain T cell activation6,7,8. Therefore, a second signal coming from the activation of the T cell surface receptor CD28 by the B7 ligands CD80 and CD86 present on APCs is needed9. During sustained activation, T cells begin to express immune checkpoint receptors like CTLA-4 that decreases the immune response by out competing CD28 for CD80 and CD86 depriving the T cell of its much needed second stimulus. Importantly, not all B7 molecules promote activation and can be suppressive. For example, the checkpoint receptor PD-1 when bound to the B7 ligand B7-H1 (PD-L1) blocks T cell proliferation, cytokine secretion and cytotoxic activity7,8. Thus, the state of T cell activation is regulated between a balance of activating and suppressive signals from immune checkpoint receptors and B7 ligands.
Discovered in 2003, B7-H4 is a member of the B7 family of co-stimulatory proteins that includes B7.1 (CD80), B7.2 (CD86), B7-H1 (CD274, PD-L1), B7-H2 (ICOS-L), B7-H3 (CD276) and B7-DC (CD273, PD-L2) that suppresses T cell proliferation and cytokine production10,11,12. Unlike other B7 proteins, B7-H4 mRNA is widely expressed in many tissues including the brain, heart, kidney, lung, ovary, pancreas and liver10. But unlike its mRNA expression, there is very little to no protein expression of B7-H4 in normal tissues13. Importantly, B7-H4 protein expression can be induced during inflammatory conditions with in vitro stimulation of cells with lipopolysaccharides, phytohemagglutinin and IFN-γ all increasing B7-H4 protein expression suggesting B7-H4 may be a valuable biomarker for the tumor microenvirnoment10.
Interest in B7-H4 as a target for treating cancer is born from the observation that it is overexpressed in both tumor cells and tumor-associated macrophages in a growing list of cancers including renal cell carcinoma13, breast cancer14, ovarian cancer15,16 and pancreatic cancer17. Furthermore, the overexpression of B7-H4 is positively associated with disease progression including cancer stage, number T cells and patient survival18,19. Given that B7-H4 suppresses T cell activation, therapeutically blocking B7-H4 signaling is hypothesized to favorably alter the tumor microenvironment allowing of T-cell targeting of cancer cells.
Taken together, while immunotherapy treatments targeting CTLA-4 and PD-L1 have been successful the fact that some patients that do not respond has created a need for new drug targets. Like PD-L1, B7-H4 is a suppressive B7 ligand that is thought to be hijacked by tumor cells to evade the immune response. Given B7-H4's ability to suppress T cell activation and its correlation for disease progression in a growing list of cancers B7-H4 may be a valuable treatment option for patients who do not respond to current immunotherapy treatments.